{"schemaVersion":"jobsearcher.job.v1","id":"12bdeba5bac4fa16eafa1e8e","url":"https://jobsearcher.com/jobs/12bdeba5bac4fa16eafa1e8e","canonicalUrl":"https://jobsearcher.com/jobs/12bdeba5bac4fa16eafa1e8e","title":"Electrical Engineer","description":"Position SummaryWe are seeking an experienced Electrical Engineer to support the design, development, testing, and regulatory compliance of medical devices. The ideal candidate will have experience supporting EU Medical Device Regulation (EU MDR 2017/745) compliance and testing against IEC 60601 series standards.Key ResponsibilitiesDesign, develop, and evaluate electrical systems and circuits for medical devices.Support EU MDR remediation activities.Plan, execute, and document electrical testing according to IEC 60601-1.Perform electrical safety testing, including:Leakage currentGround continuityDielectric withstand / HipotInsulation resistanceSingle fault condition evaluationsSupport EU MDR compliance activities.Develop and maintain MDR Technical Files and Design History Files.Collaborate with Regulatory Affairs and Quality Assurance teams.Participate in ISO 14971 risk management activities.Support EMC and electrical safety testing per IEC 60601-1-2.Interface with external test laboratories and certification bodies.Investigate product failures and implement corrective actions.Generate engineering reports, test protocols, validation documentation, and design verification reports.Required QualificationsBachelor's degree in Electrical Engineering or related engineering discipline.Minimum 3 years of experience in medical device development or a highly regulated industry.Knowledge of EU MDR 2017/745 requirements.Hands-on experience conducting and documenting testing to IEC 60601-1.Experience with electrical safety test equipment and laboratory environments.Understanding of design controls and quality systems, preferably ISO 13485.Knowledge of ISO 14971 risk management.Ability to interpret electrical schematics, technical specifications, and test requirements.Strong troubleshooting and analytical skills.Preferred QualificationsIEC 60601-1-2 / EMC testingCE marking activitiesFDA medical device regulationsVerification & validation testingEmbedded systems, power electronics, or medical device software integrationExperience with Notified Bodies and third-party test laboratories","company":"Pentangle Tech Services","rawCompany":"pentangle tech services p5 group","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-09-21T07:22:36.954Z","occupations":[{"code":"17-2071.00","title":"Electrical Engineers","slug":"electrical-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2072.00","title":"Electronics Engineers, Except Computer","slug":"electronics-engineers-except-computer"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"335999","title":"All Other Miscellaneous Electrical Equipment and Component Manufacturing","slug":"all-other-miscellaneous-electrical-equipment-and-component-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Electrical Engineer","description":"Position SummaryWe are seeking an experienced Electrical Engineer to support the design, development, testing, and regulatory compliance of medical devices. The ideal candidate will have experience supporting EU Medical Device Regulation (EU MDR 2017/745) compliance and testing against IEC 60601 series standards.Key ResponsibilitiesDesign, develop, and evaluate electrical systems and circuits for medical devices.Support EU MDR remediation activities.Plan, execute, and document electrical testing according to IEC 60601-1.Perform electrical safety testing, including:Leakage currentGround continuityDielectric withstand / HipotInsulation resistanceSingle fault condition evaluationsSupport EU MDR compliance activities.Develop and maintain MDR Technical Files and Design History Files.Collaborate with Regulatory Affairs and Quality Assurance teams.Participate in ISO 14971 risk management activities.Support EMC and electrical safety testing per IEC 60601-1-2.Interface with external test laboratories and certification bodies.Investigate product failures and implement corrective actions.Generate engineering reports, test protocols, validation documentation, and design verification reports.Required QualificationsBachelor's degree in Electrical Engineering or related engineering discipline.Minimum 3 years of experience in medical device development or a highly regulated industry.Knowledge of EU MDR 2017/745 requirements.Hands-on experience conducting and documenting testing to IEC 60601-1.Experience with electrical safety test equipment and laboratory environments.Understanding of design controls and quality systems, preferably ISO 13485.Knowledge of ISO 14971 risk management.Ability to interpret electrical schematics, technical specifications, and test requirements.Strong troubleshooting and analytical skills.Preferred QualificationsIEC 60601-1-2 / EMC testingCE marking activitiesFDA medical device regulationsVerification & validation testingEmbedded systems, power electronics, or medical device software integrationExperience with Notified Bodies and third-party test laboratories","datePosted":"2026-09-21T07:22:36.954Z","dateModified":"2026-09-21T07:22:36.954Z","hiringOrganization":{"@type":"Organization","name":"Pentangle Tech Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"12bdeba5bac4fa16eafa1e8e"},"url":"https://jobsearcher.com/jobs/12bdeba5bac4fa16eafa1e8e"}}